ClinGen Allele Registry
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Canonical Allele Identifier:
CA308127733
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.38645863G>C
Linked Data - NCBI & NCI
dbSNP:
922209638
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.38645863G>C , CM000681.2:g.38645863G>C
GRCh38
NC_000019.9:g.39136503G>C , CM000681.1:g.39136503G>C
GRCh37
NC_000019.8:g.43828343G>C
NCBI36
NG_007082.2:g.3177G>C
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